2002
DOI: 10.1007/s003960200000
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Preparation and characterization of poly ( N -isopropylacrylamide- co -dimethylaminoethyl methacrylate) microgel latexes

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Cited by 73 publications
(62 citation statements)
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“…Recently, polymer microgels are attracting much attention for their use as drug carriers, since they exhibit high water-retaining ability, biocompatibility, biodegradability, and stimuli-sensitivity (Oh et al, 2008). The stimuli-sensitivity of microgels can be obtained by introducing specific functional groups to the polymer network or using polymers which are sensitive to stimuli such as the changes in temperature, pH, or light intensity (Liu et al, 2008;Zha et al, 2002;Zhang et al, 2006;Garcia et al, 2007). Polysaccharides (e.g.…”
Section: Introductionmentioning
confidence: 99%
“…Recently, polymer microgels are attracting much attention for their use as drug carriers, since they exhibit high water-retaining ability, biocompatibility, biodegradability, and stimuli-sensitivity (Oh et al, 2008). The stimuli-sensitivity of microgels can be obtained by introducing specific functional groups to the polymer network or using polymers which are sensitive to stimuli such as the changes in temperature, pH, or light intensity (Liu et al, 2008;Zha et al, 2002;Zhang et al, 2006;Garcia et al, 2007). Polysaccharides (e.g.…”
Section: Introductionmentioning
confidence: 99%
“…Though burst release patterns are useful for certain 65 treatments, they are most often detrimental to the pharmacologi- 66 cal and economical performance of the drug delivery system [3]. 67 Chemical engineers have thus far addressed problems of drug 68 delivery control in hydrogel-based drug delivery systems by 69 designing nanodomain-structured materials, such as block copoly-70 mers, that bind to drug molecules through electrostatic [4,5] and 71 covalent bonds [6,7] as well as hydrophobic interactions [8,9], 72 delaying diffusion of the drug out of the material. More complex 73 assemblies combining electrostatic and hydrophobic interactions 74 have been developed to co-deliver hydrophilic and hydrophobic 75 drugs [10][11][12][13] to thereby trigger drug synergy or suppress drug 76 resistance.…”
mentioning
confidence: 99%
“…Attempting to increase the VPTT of a PNIPAAm chain proved successful through the incorporation of hydrophilic monomers; however this rendered the structure unusable for thermosensitive drug release systems, as it diminished the sharpness of their volume phase transition and extended the phase transition temperature range [ 70 ]. Good examples of such systems are hydrogels including PNIPAAm.…”
Section: Stimuli-responsive Nanogels In Drug Delivery Systemsmentioning
confidence: 99%